List of variants in gene MAX reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_002382.5(MAX):c.63+67G>A	rs117197166	0.03099
NM_002382.5(MAX):c.172-167del	rs140790039	0.01098
NM_002382.5(MAX):c.172-6443T>A	rs78342855	0.00675
NM_002382.5(MAX):c.172-196C>T	rs145030158	0.00673
NM_002382.5(MAX):c.171+36A>G	rs115053488	0.00564
NM_002382.5(MAX):c.172-5876C>T	rs150506672	0.00523
NM_002382.5(MAX):c.172-61C>T	rs184998980	0.00289
NM_002382.5(MAX):c.296-589A>C	rs190410205	0.00081
NM_002382.5(MAX):c.*7C>T	rs199514174	0.00051
NM_002382.5(MAX):c.171+20T>C	rs374325957	0.00003
NM_002382.5(MAX):c.172-189_172-188del	rs373737401
NM_002382.5(MAX):c.315G>A (p.Ala105=)	rs761220254
NM_002382.5(MAX):c.37-15del	rs747340873
NM_002382.5(MAX):c.435G>A (p.Glu145=)	rs1555340184

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